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United States · US · US:71288-169_bb497b35-a3a3-43e8-a187-6ad2851acf26
Cytarabine
Orange BookUNIISPLATC L01BC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMeitheal Pharmaceuticals Inc.
CountryUS (United States)
ATC codeL01BC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1171288169251 VIAL, MULTI-DOSE in 1 CARTON (71288-169-25) / 25 mL in 1 VIAL, MULTI-DOSE
Annotations
UNII (FDA Substance ID)
04079A1RDZ
CYTARABINE
RxCUI 3041
Orange Book
A208485
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "04079A1RDZ",
"rxcui": "3041",
"inchikey": "UHDGCWIWMRVCDJ-CCXZUQQUSA-N",
"display_name": "CYTARABINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS; SUBCUTANEOUS",
"spl_meta": {
"277597b0-7d85-40a3-a34a-70c6a883fc6d": {
"match": "brand_token",
"title": "CYTARABINE INJECTION, SOLUTION [HOSPIRA, INC.]",
"spl_version": "13",
"published_date": "2025-09-01"
}
},
"productid": "71288-169_bb497b35-a3a3-43e8-a187-6ad2851acf26",
"productndc": "71288-169",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "208485",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "20MG/ML",
"product_no": "001",
"approval_date": "Feb 28, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CYTARABINE",
"proprietary_name": "Cytarabine",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA208485",
"marketing_category": "ANDA",
"nonproprietary_name": "Cytarabine",
"start_marketing_date": "20220228",
"active_numerator_strength": "20"
}Related drugs
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